Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Clinical Trial

The REVIVE Pivotal Study

NCT: NCT07361653 · NOT_YET_RECRUITING

NCT IDNCT07361653
StatusNOT_YET_RECRUITING
Start Date2026-06
Completion2029-12

Brief Summary

The goal of this study is to test whether a new treatment called the Ryme Medical Targeted Lung Denervation (TLD) Catheter is safe and effective for people with moderate to severe chronic obstructive pulmonary disease (COPD). The main questions it aims to answer are: 1. Does the TLD Catheter improve symptoms in people with COPD? 2. Is the TLD Catheter safe ? Researchers will compare the group receiving the TLD treatment to the group receiving a sham procedure to see if the treatment improves quality of life. Participants will: 1. Be randomly assigned to receive either the TLD treatment or a sham procedure. 2. Undergo the assigned procedure in a hospital setting. 3. Attend follow-up visits for health checks and breathing tests.

Frequently Asked Questions

What is The REVIVE Pivotal Study?

The REVIVE Pivotal Study is a clinical trial registered under NCT07361653. Current status: NOT_YET_RECRUITING.

What is the status of NCT07361653?

The current status of NCT07361653 (The REVIVE Pivotal Study) is: NOT_YET_RECRUITING.

When did The REVIVE Pivotal Study start?

The REVIVE Pivotal Study started on 2026-06.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.